IN THE MATTER OF THE MENTAL CAPACITY ACT 2005
AND IN THE MATTER OF AG
B e f o r e :
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AG (BY HER LITIGATION FRIEND THE OFFICIAL SOLICITOR) | Applicant | |
-and- | ||
BMBC (FIRST RESPONDENT) | ||
SNH (SECOND RESPONDENT) | Respondent |
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For the Applicant: Miss A Weereratne QC
For the First Respondent: Miss F Gardner
For the Second Respondent: Mr M Wenban-Smith
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Crown Copyright ©
Background
Capacity
Best Interests
(a) the medications prescribed for covert medication purposes;(b) the reason for the covert medication plan;
(c) the details of any review; and
(d) whether the covert medication plan continued to be required.
(a) best practice regarding the review of deprivation of liberty whereby a standard authorisation has been granted for the maximum period of twelve months;(b) what constitutes a change in the relevant person's circumstances that may give rise to a variation in the condition applied to a standard authorisation; and
(c) the duty incumbent upon the managing authority in terms of updating the supervisory body.
The Evidence
(a) the council filed a statement from KL the best interests assessor on 18th February 2016;(b) the council filed its statement from PF on 22nd February 2016;
(c) the RPR (SH) filed a statement; and
(d) the home has disclosed copies of the Applicant's medication charts and notes.
Discussion
(a) Proper consideration does not appear to have been given to the initial covert use of promethazine between November 2014 and February 2015.(b) The use of covert medication in this case was not subject to proper reviews or safeguards.
(c) The decision to administer diazepam covertly in February 2015 (as prescribed by the GP) appears not to have been communicated to the supervisory body (BMBC) or to the RPR (SH) so that an opportunity to request a review of the standard authorisation at that time was lost [Schedule A!,Part8,of the Act].
(d) There does not appear to have been a review [or provision for review] of the fundamental decision to administer medication covertly notwithstanding the covert medication policy disclosed makes it clear that this is only to be considered in exceptional circumstances.
(e) The best interest decision making process appears not to have involved any family member or RPR on behalf of AG nor the social worker PF.
"1(6) Before the act is done, or the decision made, regard must be had to whether the purpose for which it is needed can be as effectively achieved in a way that is less restrictive of the person's rights and freedom of action".
Such intervention must be proportionate to the circumstances of the case and accord with the principle of minimum intervention consistent with best interests.
"Their essence is to secure professional assessment, by people independent of the hospital or care home in question, of:
(a) whether the person concerned lacks the capacity to make his own decision about whether to be accommodated in the hospital or care home for the purpose of care or treatment (paragraph 15 of Schedule A1); and
(b) whether it is in his best interest to be detained: paragraph 16. The procedures are administrative but the authorisation can be challenged in the Court of Protection under Section 21A."
"When a person is deprived of their liberty, the managing authority has a duty to monitor the case on an ongoing basis to see if the person's circumstances change – which may mean they no longer need to be deprived of their liberty. The managing authority must set out in the care plan clear roles and responsibilities for monitoring and confirm under what circumstances a review is necessary. For example if a person's condition is changing frequently, then their situation should be reviewed more frequently."
Conclusions
(a) all administration of covert medication is subject to the appropriate safeguards; and(b) there is clear communication and an understanding of what is expected between the supervisory body and the managing authorities in circumstances where a person is deprived of their liberty and their care plan includes the administration of covert medication.
(1) The length of a standard authorisation.
That to a large degree is fact specific. Alternate medication, similar in prescription, may not do so; a change in prescription in strength/dosage nature and effect will almost certainly do so. In this particular case the change in medication in February 2015 (diazepam being a stronger form of medication) should have triggered a review, it being a change to the care plan and revision to the covert medication known at the time the authorisation was given.
What of course flows from this is that the original best interest decision must be clear and there must be a proper and fully recorded care plan and review process which in the event of change of circumstance can be triggered. In turn that information must be easily and readily accessible not only to the healthcare professionals but also to those who may be representing P. Clearly any change to the care plan should be notified promptly by the managing authority to the supervisory body.
(i) if a person lacks capacity and is unable to understand the risks to their health if they do not take their prescribed mediation and the person is refusing to take the medication then it should only be administered covertly in exceptional circumstances;(ii) before the medication is administered covertly there must be a best interest decision which includes the relevant health professionals and the person's family members;
(iii) if it is agreed that the administration of covert medication is in their best interests then this must be recorded and placed in the person's medical records/care home records and there must be an agreed management plan including details of how it is to be reviewed; and
(iv) all of the above documentation must be easily accessible on any viewing of the person's records within the care/nursing home.
(v) If there is no agreement then there should be an immediate application to Court
Summary
(a) Where there is a covert medication policy in place or indeed anything similar there must be full consultation with healthcare professionals and family.(b) The existence of such treatment must be clearly identified within the assessment and authorisation.
(c) If the standard authorisation is to be for a period of longer than six months there should be a clear provision for regular, possibly monthly, reviews of the care and support plan.
(d) There should at regular intervals be review involving family and healthcare professionals, all the more so if the standard authorisation is to be for the maximum twelve month period.
(e) Each case must be determined on its facts but I cannot see that it would be sensible for there to be an absolute policy that, in circumstances similar to this, standard authorisation should be limited to six months. It may be perfectly practical and proportionate provided there is a provision for reviews(or conditions attached) for the standard authorisation to be for the maximum period.
(f) Where appointed an RPR should be fully involved in those discussions and review so that if appropriate an application for part 8 review can be made.
(g) Any change of medication or treatment regime should also trigger a review where such medication is covertly administered.
(h) Such matters can be achieved by placing appropriate conditions to which the standard authorisation is subject and would of course accord with chapter 8 of the deprivation of liberty safeguard's code of practice.
(i) I endorse and gratefully adopt the proposed written guidance from BMBC as detailed earlier in this judgment and, whilst recognising it may not be proportionate or indeed desirable in every case, the revised format of the most recent standard authorisation.
Dated this 6 day of July 2016
District Judge Bellamy